Ear Pain MD

openFDA label record#

This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.

Verified complete openFDA source JSON (canonical bytes are SHA-256 checked before publication)

Brand name: Ear Pain MD
Generic name: LIDOCAINE HYDROCHLORIDE
Manufacturer: Eosera Inc
Product type: HUMAN OTC DRUG
SPL set ID: 78c4418f-7f0f-447f-a94f-d4c89a081af1
SPL ID: afe9f614-c9f1-484f-8419-9c7bd6db7084
Version: 5
Effective date: 2025-10-17
Source export date: 2026-10-12
Source partition: 2
Source file: https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/4760f38f2bcb10aa20ddbadb42b270d31e9f2a8024440d3af3dec8d11feb92ec/drug-label-0002-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 01:27:32

Harmonized routes table
Harmonized routes
TOPICAL

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 19 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
application number		M017	openfda.application_number
brand name		Ear Pain MD	openfda.brand_name
brand name		Ear Pain MD for Kids	openfda.brand_name
generic name		LIDOCAINE HYDROCHLORIDE	openfda.generic_name
manufacturer name		Eosera Inc	openfda.manufacturer_name
ndc	package	72429-0002-9	openfda.package_ndc
ndc	package	72429-0001-8	openfda.package_ndc
ndc	package	72429-0001-9	openfda.package_ndc
ndc	package	72429-0002-8	openfda.package_ndc
ndc	product	72429-0002	openfda.product_ndc
ndc	product	72429-0001	openfda.product_ndc
ndc11	package	72429000209	derived:openfda.package_ndc
ndc11	package	72429000109	derived:openfda.package_ndc
ndc11	package	72429000208	derived:openfda.package_ndc
ndc11	package	72429000108	derived:openfda.package_ndc
rxcui		2595042	openfda.rxcui
spl id		afe9f614-c9f1-484f-8419-9c7bd6db7084	id
spl set id		78c4418f-7f0f-447f-a94f-d4c89a081af1	set_id
unii		V13007Z41A	openfda.unii

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings Keep out of reach of children. For external use only. If swallowed, immediately call Poison Control 800-222-1222. Avoid contact with the eyes. Do not use in large quantities, particularly over raw surfaces or blistered areas. if you are allergic to any ingredient in this product. if you have an injury or perforation (hole) of the eardrum or tubes in the ear. If conditions worsen, or if symptoms persist for more than 7 days or clear up and occur again within a few days, discontinue use of this product and consult a doctor.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.